Canonical Allele Identifier: CA2250822512

Gene: ATPAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18021072G= , CM000679.2:g.18021072G=	GRCh38
NC_000017.10:g.17924386G= , CM000679.1:g.17924386G=	GRCh37
NC_000017.9:g.17865111G=	NCBI36
NG_012824.1:g.23095C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474627.8:c.732+51C= MANE Select	ENSP00000417190.2:n.732+51C=
ENST00000462733.5:c.*149+51C=	ENSP00000463920.1:n.*149+51C=
ENST00000465337.2:n.591+51C=
ENST00000467560.5:n.142+51C=
ENST00000469327.5:n.642+51C=
ENST00000474627.7:c.732+51C=	ENSP00000417190.2:n.732+51C=
ENST00000488753.1:n.527+51C=
ENST00000496852.5:n.1237+51C=
ENST00000581698.1:c.49-2386C=
ENST00000584205.5:c.*33+3552C=	ENSP00000462899.1:n.*33+3552C=
ENST00000585101.5:c.*33+3552C=	ENSP00000463861.1:n.*33+3552C=
NM_145691.3:c.732+51C=	NP_663729.1:n.732+51C=
XM_005256848.2:c.732+51C=	XP_005256905.1:n.732+51C=
XM_011524062.1:c.732+51C=	XP_011522364.1:n.732+51C=
XM_011524063.1:c.732+51C=	XP_011522365.1:n.732+51C=
XM_011524064.1:c.432+51C=	XP_011522366.1:n.432+51C=
XM_011524065.1:c.732+51C=	XP_011522367.1:n.732+51C=
XM_011524066.1:c.195+51C=	XP_011522368.1:n.195+51C=
XM_005256848.4:c.732+51C=	XP_005256905.1:n.732+51C=
XM_011524065.2:c.732+51C=	XP_011522367.1:n.732+51C=
XM_017025302.1:c.432+51C=	XP_016880791.1:n.432+51C=
XM_017025303.1:c.432+51C=	XP_016880792.1:n.432+51C=
XR_001752677.2:n.1129+51C=
NM_145691.4:c.732+51C= MANE Select	NP_663729.1:n.732+51C=